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FEBS Letters
|
June 8, 2001
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene
J Klepper, I Monden, E Guertsen, et al.
Annals of Neurology
|
May 19, 2001
Hypoglycorrhachia: a simple clue, simply missed
M A Willemsen, A Verrips, M M Verbeek, et al.
Clinical Neuropathology
|
November 1, 1987
Neonatal myotonic dystrophy in a premature infant: clinical and morphological findings
E Neuen-Jacob, T Voit, J Turski, et al.
The American Journal of Pathology
|
November 1, 1991
Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodies
T Voit, K Haas, J O Léger, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles
F Pons, L V Nicholson, A Robert, et al.
Neurology
|
July 23, 1998
Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases
R D Cohn, R Herrmann, L Sorokin, et al.
Neurology
|
February 12, 2004
Respiratory function in congenital muscular dystrophy and limb girdle muscular dystrophy 2I
C Dohna-Schwake, R Ragette, U Mellies, et al.
The New England Journal of Medicine
|
September 14, 1995
Serum antibodies to the deleted dystrophin sequence after cardiac transplantation in a patient with Becker's muscular dystrophy
R E Bittner, S Shorny, B Streubel, et al.
The European Respiratory Journal
|
October 30, 2003
Long-term noninvasive ventilation in children and adolescents with neuromuscular disorders
U Mellies, R Ragette, C Dohna Schwake, et al.
Neurology
|
April 27, 2005
Respiratory failure in Pompe disease: treatment with noninvasive ventilation
U Mellies, F Stehling, C Dohna-Schwake, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 143) with videos related to
Sort By:
Page
of 15
FEBS Letters
|
June 8, 2001
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene
J Klepper, I Monden, E Guertsen, et al.
Annals of Neurology
|
May 19, 2001
Hypoglycorrhachia: a simple clue, simply missed
M A Willemsen, A Verrips, M M Verbeek, et al.
Clinical Neuropathology
|
November 1, 1987
Neonatal myotonic dystrophy in a premature infant: clinical and morphological findings
E Neuen-Jacob, T Voit, J Turski, et al.
The American Journal of Pathology
|
November 1, 1991
Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodies
T Voit, K Haas, J O Léger, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles
F Pons, L V Nicholson, A Robert, et al.
Neurology
|
July 23, 1998
Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases
R D Cohn, R Herrmann, L Sorokin, et al.
Neurology
|
February 12, 2004
Respiratory function in congenital muscular dystrophy and limb girdle muscular dystrophy 2I
C Dohna-Schwake, R Ragette, U Mellies, et al.
The New England Journal of Medicine
|
September 14, 1995
Serum antibodies to the deleted dystrophin sequence after cardiac transplantation in a patient with Becker's muscular dystrophy
R E Bittner, S Shorny, B Streubel, et al.
The European Respiratory Journal
|
October 30, 2003
Long-term noninvasive ventilation in children and adolescents with neuromuscular disorders
U Mellies, R Ragette, C Dohna Schwake, et al.
Neurology
|
April 27, 2005
Respiratory failure in Pompe disease: treatment with noninvasive ventilation
U Mellies, F Stehling, C Dohna-Schwake, et al.
Page
of 15